{{Rsnum
|rsid=929156
|Gene=TRIM15
|Chromosome=6
|position=30171922
|Orientation=minus
|GMAF=0.2006
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TRIM15
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 42.5 | 46.0 | 11.5
| HCB | 57.7 | 36.5 | 5.8
| JPT | 73.5 | 24.8 | 1.8
| YRI | 83.0 | 15.6 | 1.4
| ASW | 78.9 | 19.3 | 1.8
| CHB | 57.7 | 36.5 | 5.8
| CHD | 52.3 | 42.2 | 5.5
| GIH | 84.2 | 14.9 | 1.0
| LWK | 87.3 | 10.9 | 1.8
| MEX | 65.5 | 32.8 | 1.7
| MKK | 85.9 | 13.5 | 0.6
| TSI | 66.7 | 31.4 | 2.0
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs929156
|Name_s=
|Gene_s=TRIM15
|Feature=
|Evidence=PubMed ID:19118814
|Annotation=This variant is significantly associated with late-onset Alzheimer disease (LOAD) in a GWAS study with 492 LOAD cases and 498 cognitive controls using Illumina's HumanHap550 beadchip.
|Drugs=
|Drug Classes=
|Diseases=Alzheimer Disease
|Curation Level=Curated
|PharmGKB Accession ID=PA162363819
}}

{{PMID Auto
|PMID=19010793
|Title=Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.
}}

{{GET Evidence
|gene=TRIM15
|aa_change=Ser324Asn
|aa_change_short=S324N
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs929156
|overall_frequency_n=1361
|overall_frequency_d=7508
|overall_frequency=0.181273
|n_genomes=11
|n_genomes_annotated=0
|n_haplomes=12
|n_articles=1
|n_articles_annotated=1
|in_pharmgkb=Y
|nblosum100=0
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}